caffeine has been researched along with Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis in 1 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Most patients with Alpers syndrome have been found to be compound heterozygotes, carrying two pathogenic mutations in trans at the POLG locus." | 1.33 | Mono-allelic POLG expression resulting from nonsense-mediated decay and alternative splicing in a patient with Alpers syndrome. ( Chan, SS; Copeland, WC; Longley, MJ; Naviaux, RK, 2005) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chan, SS | 1 |
| Longley, MJ | 1 |
| Naviaux, RK | 1 |
| Copeland, WC | 1 |
1 other study available for caffeine and Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis
| Article | Year |
|---|---|
Mono-allelic POLG expression resulting from nonsense-mediated decay and alternative splicing in a patient with Alpers syndrome.
Topics: Alleles; Alternative Splicing; Amino Acid Sequence; Androstadienes; Caffeine; Child, Preschool; Codo | 2005 |